neuroblastoma cure rate

Written by Chen Yu Fei
Neurosurgery
Updated on November 17, 2024
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Neuroblastoma is relatively likely to be a malignant tumor, typically characterized by rapid growth of malignant tumors.

In the early stages of the disease, it often adheres to surrounding tissues, making it difficult to completely remove through surgery. Even with surgical treatment, the outcomes are generally modest, and recurrence is likely to occur shortly after surgery. Once recurrence occurs, the malignancy of the tumor will continue to increase.

For these patients, the prognosis is poor. It is generally recommended to undergo surgical treatment early, followed by radiotherapy and chemotherapy to potentially extend the patient's lifespan, but it is usually difficult to cure.

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Written by Chen Yu Fei
Neurosurgery
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Neuroblastoma is what disease

Neuroblastoma is a highly malignant epithelial neurocyte tissue tumor, which is relatively aggressive. Often in the early stages of the disease, the tumor tissue adheres to surrounding brain tissue, nerves, and blood vessels, making it impossible to completely remove it surgically. The residual tumor cells quickly recur over time. As a result, most neuroblastoma patients have a poor prognosis and short survival time, even with effective surgical treatment, including postoperative radiotherapy and chemotherapy. Therefore, it is recommended that those diagnosed with neuroblastoma undergo early further examinations and treatments.

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home-news-image
Written by Chen Yu Fei
Neurosurgery
42sec home-news-image

neuroblastoma cure rate

Neuroblastoma is relatively likely to be a malignant tumor, typically characterized by rapid growth of malignant tumors.In the early stages of the disease, it often adheres to surrounding tissues, making it difficult to completely remove through surgery. Even with surgical treatment, the outcomes are generally modest, and recurrence is likely to occur shortly after surgery. Once recurrence occurs, the malignancy of the tumor will continue to increase.For these patients, the prognosis is poor. It is generally recommended to undergo surgical treatment early, followed by radiotherapy and chemotherapy to potentially extend the patient's lifespan, but it is usually difficult to cure.

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home-news-image
Written by Chen Yu Fei
Neurosurgery
44sec home-news-image

How is neuroblastoma diagnosed?

For patients with neuroblastoma, diagnosis is primarily through the symptoms, signs, detailed physical examinations, medical history inquiries, and most importantly, radiological data, which includes CT scans or MRI of the head. Definitive diagnosis requires surgical removal of the tumor. A small amount of tumor tissue is retained after excision and used for pathological examination to confirm the diagnosis. Neuroblastoma is categorized as an epithelial-like malignant tumor, indicative of a high degree of malignancy. In most cases, early in the disease, the tumor adheres to surrounding tissues, which greatly complicates complete surgical removal, and most patients have a poor prognosis.

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Written by Chen Yu Fei
Neurosurgery
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Age of onset of neuroblastoma

Neuroblastoma, typically arises from primitive neural crest cells, is more commonly found in the sympathetic ganglia and adrenal medulla. There is no specific age for the onset of neuroblastoma, but research indicates that it is more commonly diagnosed in children. The exact causative factors of neuroblastoma are not yet fully understood, but it is widely believed to involve congenital genetic factors, including acquired genetic mutations. Clinically, the presentation largely depends on the location of the tumor, the age at diagnosis, and the degree of malignancy of the tumor. In most cases, the tumor originates in the abdominal cavity, with a higher occurrence in the adrenal glands in children.

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Written by Chen Yu Fei
Neurosurgery
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Neuroblastoma examination items

For neuroblastoma, the examination items mainly include the patient's vital signs and physical examination, including detailed examinations to observe if there are any obvious pathological signs. Additionally, it is necessary to inquire about the patient’s medical history, especially past medical history and family history. Main examination items include laboratory tests, routine blood and urine tests, biochemistry, and tumor-related tests. Furthermore, examinations also involve using a cranial CT scan, MRI of the head, and if necessary, an enhanced MRI scan of the head, to further determine the presence of neuroblastoma, as well as its location, quantity, and the relationship between the surrounding tissues, blood vessels, and nerves.